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Links from GEO DataSets

Items: 9

1.

APOL1 renal-risk variants induce mitochondrial dysfunction

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL10558 GPL17586
60 Samples
Download data: CEL, IDAT
Series
Accession:
GSE85921
ID:
200085921
2.

APOL1 renal-risk variants induce mitochondrial dysfunction (Affymetrix 2)

(Submitter supplied) To assess differential gene expression by APOL1 renal-risk (2 risk alleles) vs. non-risk (G0G0) genotypes in primary proximal tubule cells (PTCs), global gene expression (mRNA) levels were examined on Affymetrix HTA 2.0 arrays in primary PTCs cultured from non-diseased kidney in African Americans without CKD who underwent nephrectomy for localized renal cell carcinoma.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
30 Samples
Download data: CEL
Series
Accession:
GSE85920
ID:
200085920
3.

APOL1 renal-risk variants induce mitochondrial dysfunction (Affymetrix 1)

(Submitter supplied) To elucidate pathways whereby apolipoprotein L1 gene (APOL1) G1 and G2 variants facilitate kidney disease in African Americans, human embryonic kidney cells (HEK293) were used to establish doxycycline-inducible (Tet-on) cell lines stably expressing reference APOL1 G0 and its G1 and G2 renal-risk variants. Illumina human HT-12-v4 arrays and Affymetrix HTA 2.0 arrays were employed to generate global gene expression data with doxycycline induction. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
6 Samples
Download data: CEL
Series
Accession:
GSE85919
ID:
200085919
4.

APOL1 renal-risk variants induce mitochondrial dysfunction (Illumina)

(Submitter supplied) To elucidate pathways whereby apolipoprotein L1 gene (APOL1) G1 and G2 variants facilitate kidney disease in African Americans, human embryonic kidney cells (HEK293) were used to establish doxycycline-inducible (Tet-on) cell lines stably expressing reference APOL1 G0 and its G1 and G2 renal-risk variants. Illumina human HT-12-v4 arrays and Affymetrix HTA 2.0 arrays were employed to generate global gene expression data with doxycycline induction. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
24 Samples
Download data: IDAT, TXT
Series
Accession:
GSE85918
ID:
200085918
5.

APOL1 variant expression in mouse podocytes cause kidney disease

(Submitter supplied) Next-generation sequencing (NGS) has become an important tool in molecular charactarization of animal models. APOL1 variants are associated with end stage renal disease in African Americans. We developed a mouse model with podocyte specific over expression of APOL1. Differential molecular signatures were identified between the groups by RNA-Sequencing on kidney.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
10 Samples
Download data: TXT
Series
Accession:
GSE81492
ID:
200081492
6.

Integrative genomics identifies novel associations with APOL1 risk genotype in African American NEPTUNE subjects

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17692
99 Samples
Download data: CEL
Series
Accession:
GSE68127
ID:
200068127
7.

Integrative genomics identifies novel associations with APOL1 risk genotype in African American NEPTUNE subjects [tubulointerstitium]

(Submitter supplied) Tubulointersitial expression data from human kidney biopsy in African American subjects with glomerulopathies We used microarrays to analyze the transcriptome of African American subjects with glomerulopathies and the association of expression with APOL1 risk alleles (G1 and G2)
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17692
55 Samples
Download data: CEL, TXT
Series
Accession:
GSE68126
ID:
200068126
8.

Integrative genomics identifies novel associations with APOL1 risk genotype in African American NEPTUNE subjects [glomerulus]

(Submitter supplied) Glomerular expression data from human kidney biopsy in African American subjects with glomerulopathies We used microarrays to analyze the transcriptome of African American subjects with glomerulopathies and the association of expression with APOL1 risk alleles (G1 and G2)
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17692
44 Samples
Download data: CEL, TXT
Series
Accession:
GSE68125
ID:
200068125
9.

Single-Cell Transcriptomics of Genome-Edited Kidney Organoids

(Submitter supplied) We report the first use of genome-edited human kidney organoids, combined with single-cell transcriptomics, to study APOL1 risk variants at the native genomic locus in different nephron cell types. This approach captures interferon-mediated induction of APOL1 gene expression and cellular dedifferentiation with a secondary insult“second hit” of endoplasmic reticulum stress.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
16 Samples
Download data: TSV
Series
Accession:
GSE135663
ID:
200135663
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